Canonical Allele Identifier: CA363497041

Gene: C2

Linked Data

• MyVariant Identifiers: chr6:g.31901655T>G (hg19) ; chr6:g.31933878T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31933878T>G , CM000668.2:g.31933878T>G	GRCh38
NC_000006.11:g.31901655T>G , CM000668.1:g.31901655T>G	GRCh37
NC_000006.10:g.32009634T>G	NCBI36
NG_011730.1:g.11390T>G , LRG_26:g.11390T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000447952.7:c.442T>G	ENSP00000391354.3:p.Tyr148Asp
ENST00000452323.7:c.259T>G	ENSP00000392322.2:p.Tyr87Asp
ENST00000468407.2:c.628T>G	ENSP00000512075.1:p.Tyr210Asp
ENST00000497706.6:c.123T>G	ENSP00000417482.2:p.Leu41=
ENST00000695637.1:c.223T>G	ENSP00000512074.1:p.Tyr75Asp
ENST00000695638.1:c.628T>G	ENSP00000512076.1:p.Tyr210Asp
ENST00000695639.1:n.431T>G
ENST00000695640.1:n.566T>G
ENST00000695644.1:c.232T>G	ENSP00000512079.1:p.Tyr78Asp
ENST00000299367.10:c.628T>G MANE Select	ENSP00000299367.5:p.Tyr210Asp
ENST00000299367.9:c.628T>G	ENSP00000299367.5:p.Tyr210Asp
ENST00000383177.7:c.222T>G
ENST00000411571.6:c.123T>G	ENSP00000388727.2:p.Leu41=
ENST00000418949.6:c.628T>G	ENSP00000406190.2:p.Tyr210Asp
ENST00000442278.6:c.232T>G	ENSP00000395683.2:p.Tyr78Asp
ENST00000447952.6:c.442T>G	ENSP00000391354.2:p.Tyr148Asp
ENST00000452202.5:c.259T>G	ENSP00000406121.1:p.Tyr87Asp
ENST00000452323.6:c.259T>G	ENSP00000392322.2:p.Tyr87Asp
ENST00000456570.5:c.442T>G	ENSP00000410815.1:p.Tyr148Asp
ENST00000469372.5:c.111+95T>G	ENSP00000418923.1:n.111+95T>G
ENST00000477310.1:c.443-3441T>G	ENSP00000418996.1:n.443-3441T>G
ENST00000482060.5:c.*341T>G	ENSP00000418332.1:n.*341T>G
ENST00000484636.1:c.123T>G	ENSP00000420305.1:p.Leu41=
ENST00000494905.1:c.205T>G	ENSP00000419048.1:p.Tyr69Asp
ENST00000497706.5:c.123T>G	ENSP00000417482.1:p.Leu41=
NM_000063.5:c.628T>G	NP_000054.2:p.Tyr210Asp
NM_001145903.2:c.232T>G	NP_001139375.1:p.Tyr78Asp
NM_001178063.2:c.259T>G	NP_001171534.1:p.Tyr87Asp
NM_001282457.1:c.111+95T>G	NP_001269386.1:n.111+95T>G
NM_001282458.1:c.541T>G	NP_001269387.1:p.Tyr181Asp
NM_001282459.1:c.628T>G	NP_001269388.1:p.Tyr210Asp
NM_000063.6:c.628T>G MANE Select	NP_000054.2:p.Tyr210Asp
NM_001145903.3:c.232T>G	NP_001139375.1:p.Tyr78Asp
NM_001282457.2:c.111+95T>G	NP_001269386.1:n.111+95T>G
NM_001282458.2:c.541T>G	NP_001269387.1:p.Tyr181Asp
NM_001282459.2:c.628T>G	NP_001269388.1:p.Tyr210Asp
NM_001178063.3:c.259T>G	NP_001171534.1:p.Tyr87Asp